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Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
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Repository for lectin-assisted multimodality data
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MIRAGE
Alliance of Genome Resources
Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.
| Source | Last Updated |
|---|---|
| Alliance of Genome Resources | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▲ | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0070145 | hereditary sensory and autonomic neuropathy type 5 | HGNC:7808 | Homo sapiens (human) | 4803 | NGF |
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| DOID:10487 | Hirschsprung's disease | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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| DOID:2531 | hematologic cancer | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0060656 | autosomal recessive congenital ichthyosis 1 | HGNC:14637 | Homo sapiens (human) | 26154 | ABCA12 |
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| DOID:1580 | diffuse scleroderma | HGNC:43 | Homo sapiens (human) | 6890 | TAP1 |
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| DOID:9119 | acute myeloid leukemia | HGNC:13013 | Homo sapiens (human) | 7994 | KAT6A |
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| DOID:8924 | autoimmune thrombocytopenic purpura | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:3312 | bipolar disorder | HGNC:4077 | Homo sapiens (human) | 2556 | GABRA3 |
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| DOID:0111834 | X-linked reticulate pigmentary disorder | HGNC:9173 | Homo sapiens (human) | 5422 | POLA1 |
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| DOID:1324 | lung cancer | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:0112167 | autosomal dominant nonsyndromic deafness 76 | HGNC:9090 | Homo sapiens (human) | 5357 | PLS1 |
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| DOID:302 | substance abuse | HGNC:11050 | Homo sapiens (human) | 6532 | SLC6A4 |
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| DOID:3008 | invasive ductal carcinoma | HGNC:7739 | Homo sapiens (human) | 4747 | NEFL |
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| DOID:0050830 | peripheral artery disease | HGNC:18124 | Homo sapiens (human) | 64805 | P2RY12 |
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| DOID:0080736 | Ehlers-Danlos syndrome musculocontractural type 1 | HGNC:24464 | Homo sapiens (human) | 113189 | CHST14 |
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| DOID:2738 | pseudoxanthoma elasticum | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:3910 | lung adenocarcinoma | HGNC:3432 | Homo sapiens (human) | 2066 | ERBB4 |
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| DOID:0110178 | Charcot-Marie-Tooth disease axonal type 2V | HGNC:7632 | Homo sapiens (human) | 4669 | NAGLU |
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| DOID:3008 | invasive ductal carcinoma | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:2738 | pseudoxanthoma elasticum | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:896 | metal metabolism disorder | HGNC:17995 | Homo sapiens (human) | 140803 | TRPM6 |
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| DOID:0070482 | spinal neurofibromatosis | HGNC:7765 | Homo sapiens (human) | 4763 | NF1 |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:11849 | Homo sapiens (human) | 7098 | TLR3 |
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| DOID:0080986 | Ehlers-Danlos syndrome periodontal type 1 | HGNC:1246 | Homo sapiens (human) | 715 | C1R |
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| DOID:234 | colon adenocarcinoma | HGNC:11366 | Homo sapiens (human) | 6776 | STAT5A |
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